4.6 Article

Anodic deposition of NiOx water oxidation catalysts from macrocyclic nickel(II) complexes

Journal

CATALYSIS SCIENCE & TECHNOLOGY
Volume 3, Issue 7, Pages 1725-1732

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cy00017f

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Funding

  1. Australian Research Council (ARC) through the Australian Centre of Excellence for Electromaterials Science (ACES)
  2. Monash University Center for Electron Microscopy
  3. Monash University

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Molecular complexes have been found to be excellent precursors for the deposition of catalytically active metal oxide films. Here, three macrocyclic Ni(II) amine complexes have been used for the electrochemical deposition of NiOx films from either a borate buffer solution (pH 9.2) or more basic conditions (pH = 12.9). The cyclic voltammetry of the complexes in both electrolytes shows very similar features and indicates the deposition of a catalytically active nickel oxide film. The NiOx films have been characterised using infrared (IR) and Raman spectroscopy complemented by scanning electron microscopy. Testing of the water oxidation activity at pH 9.2 and 12.9 showed that the films deposited from macrocyclic Ni(II) complexes exhibit similar catalytic activity to those derived from Ni2+ salts. The macrocyclic complexes offer the advantage of greater solubility and solution stability over a wider range of deposition conditions. At pH 9.2, the catalytic activity of the NiOx films was significantly higher when using a borate buffer and, in addition, the films were more active at pH 12.9 than at pH 9.2. The NiOx films deposited from molecular complexes were also found to show electrochromic properties. The oxidation of water by these films was enhanced by visible light. Water oxidation currents were observed to increase by similar to 20% under simulated solar radiation.

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